Anna Helgadóttir

Active 2004–2025

Also published as
Anna Helgadottir
68
Papers
20,255
Citations
51
h-index
65
i10-index

Citations

Citations per year for Anna Helgadóttir1974: 1 citations1982: 1 citations1986: 1 citations1998: 1 citations2000: 1 citations2002: 1 citations2004: 18 citations2005: 32 citations2006: 86 citations2007: 139 citations2008: 178 citations2009: 260 citations2010: 289 citations2011: 248 citations2012: 255 citations2013: 212 citations2014: 175 citations2015: 168 citations2016: 138 citations2017: 158 citations2018: 119 citations2019: 329 citations2020: 401 citations2021: 462 citations2022: 460 citations2023: 461 citations2024: 772 citations2025: 394 citations2026: 40 citations1975–1981: no citations, so these years are not shown1983–1985: no citations, so these years are not shown1987–1997: no citations, so these years are not shown1999: no citations, so this year is not shown2001: no citations, so this year is not shown2003: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,562 citing papers, 21.4% of this breakdownUnited Kingdom: 1,166 citing papers, 9.8% of this breakdownChina: 843 citing papers, 7% of this breakdownGermany: 664 citing papers, 5.6% of this breakdownNetherlands: 525 citing papers, 4.4% of this breakdownCanada: 486 citing papers, 4.1% of this breakdownSweden: 449 citing papers, 3.8% of this breakdownItaly: 411 citing papers, 3.4% of this breakdownAustralia: 378 citing papers, 3.2% of this breakdownFrance: 338 citing papers, 2.8% of this breakdownDenmark: 328 citing papers, 2.7% of this breakdownFinland: 299 citing papers, 2.5% of this breakdown
0%21.4%Other 29.3%

Fields

  • Biochemistry, Genetics and Molecular Biology46.7%
  • Medicine42.4%
  • Immunology and Microbiology4.4%
  • Neuroscience2.3%
  • Nursing0.9%
  • Computer Science0.8%
  • Other2.5%

Topics

  • Genetic Associations and Epidemiology11.1%
  • Lipoproteins and Cardiovascular Health2.3%
  • Genetic Mapping and Diversity in Plants and Animals2.2%
  • Bioinformatics and Genomic Networks2.1%
  • Pancreatic function and diabetes1.9%
  • Epigenetics and DNA Methylation1.9%
  • Other78.5%

Coauthors

All papers

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  1. The power of genetic diversity in genome-wide association studies of lipids

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Masato Akiyama, Saori Sakaue, Chikashi Terao, Masahiro Kanai, Wei Zhou, Ben Brumpton, Humaira Rasheed, Sanni Ruotsalainen, Aki S. Havulinna, Yogasudha Veturi, QiPing Feng, Elisabeth A. Rosenthal, Todd Lingren, Jennifer A. Pacheco, Sarah A. Pendergrass, Jeffrey Haessler, Franco Giulianini, Yuki Bradford, Jason E. Miller, Archie Campbell, Kuang Lin, Iona Y. Millwood, George Hindy, Asif Rasheed, Jessica D. Faul, Wei Zhao, David R. Weir, Constance Turman, Hongyan Huang, Mariaelisa Graff, Anubha Mahajan, Michael R. Brown, Weihua Zhang, Ketian Yu, Ellen M. Schmidt, Anita Pandit, Stefan Gustafsson, Xianyong Yin, Jian’an Luan, Jing-Hua Zhao, Fumihiko Matsuda, Hye-Mi Jang, Kyungheon Yoon, Carolina Medina‐Gómez, Achilleas Pitsillides, Jouke‐Jan Hottenga, Gonneke Willemsen, Andrew R. Wood, Yingji Ji, Zishan Gao, Simon Haworth, Ruth E. Mitchell, Jin Fang Chai, Mette Aadahl, Jie Yao, Ani Manichaikul, Helen R. Warren, Julia Ramírez, Jette Bork‐Jensen, Line Lund Kårhus, Anuj Goel, Maria Sabater‐Lleal, Raymond Noordam, Carlo Sidore, Edoardo Fiorillo, Aaron F. McDaid, Pedro Marques‐Vidal, Matthias Wielscher, Stella Trompet, Naveed Sattar and 427 more - Nature 2021 cited by 1,079

  2. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Adnan Kastrati, Thorsten Kessler, Theodosios Kyriakou, Tomasz Konopka, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B. Nielsen, Markus M. Nöthen, Shichao Pang, Tobias Reinberger, Gavin R. Schnitzler, Damian Smedley, Guðmar Þorleifsson, Moritz von Scheidt, Jacob C. Ulirsch, Biobank Japan, EPIC-CVD, John Danesh, Davíð O. Arnar, Noël P. Burtt, Maria C. Costanzo, Jason Flannick, Kaoru Ito, Dongkeun Jang, Yoichiro Kamatani, Amit V. Khera, Issei Komuro, Iftikhar J. Kullo, Luca A. Lotta, Christopher P. Nelson, Robert Roberts, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Tom R. Webb, Aris Baras, Johan Björkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C. Morrison, Marju Orho‐Melander, Lοukianos S. Rallidis, Arno Ruusalepp, Marc S. Sabatine, Kāri Stefánsson, Pierre Zalloua, Patrick T. Ellinor, Martin Farrall, John Danesh, Christian T. Ruff, Hilary K. Finucane, Jemma C. Hopewell, Robert Clarke, Rajat M. Gupta, Jeanette Erdmann, Nilesh J. Samani, Heribert Schunkert, Hugh Watkins, Cristen J. Willer, Panos Deloukas, Sekar Kathiresan, Adam S. Butterworth, Paul S. de Vries, Moritz von Scheidt - Nature Genetics 2022 cited by 706

  3. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Graciela E. Delgado, Spiros Denaxas, Alex S. F. Doney, Marcus Dörr, Samuel C. Dudley, Michael E. Dunn, Gunnar Engström, Tõnu Esko, Stephan B. Felix, Chris Finan, Ian Ford, Mohsen Ghanbari, Sahar Ghasemi, Vilmantas Giedraitis, Franco Giulianini, John S. Gottdiener, Stefan Groß, Daníel F. Guðbjartsson, Rebecca Gutmann, Christopher M. Haggerty, Pim van der Harst, Craig Hyde, Erik Ingelsson, J. Wouter Jukema, Maryam Kavousi, Kay‐Tee Khaw, Marcus E. Kleber, Lars Køber, Andrea Koekemoer, Claudia Langenberg, Lars Lind, Cecilia M. Lindgren, Barry London, Luca A. Lotta, Ruth C. Lovering, Jian’an Luan, Patrik K. E. Magnusson, Anubha Mahajan, Kenneth B. Margulies, Winfried März, Olle Melander, Ify Mordi, Thomas M. Morgan, Andrew D. Morris, Andrew P. Morris, Alanna C. Morrison, Michael W. Nagle, Christopher P. Nelson, Alexander Niessner, Teemu Niiranen, Michelle L. O’Donoghue, Anjali Owens, Colin N. A. Palmer, Helen Parry, Markus Perola, Eliana Portilla-Fernández, Bruce M. Psaty, Goncalo Abecasis, Joshua Backman, Xiaodong Bai, Suganthi Balasubramanian, Nilanjana Banerjee, Aris Baras, Leland Barnard, Christina Beechert, Andrew Blumenfeld, Michael Cantor, Yating Chai, Jonathan Chung, Giovanni Coppola and 103 more - Nature Communications 2020 cited by 929

  4. Multiomics study of nonalcoholic fatty liver disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Valgerður Steinthórsdóttir, Michael Schwinn, Guðmundur Þorgeirsson, Guðmar Þorleifsson, Ingileif Jónsdóttir, Henning Bundgaard, Lincoln Nadauld, Einar S. Björnsson, Ingrid C. Rulifson, Þórunn Rafnar, Gudmundur L. Norddahl, Unnur Þorsteinsdóttir, Patrick Sulem, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson - Nature Genetics 2022 cited by 229

  5. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2006 cited by 2,279

  6. Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alex Hørby Christensen, Susan Mikkelsen, Rikke Louise Jacobsen, Joseph Dowsett, Ole Birger Pedersen, Christian Erikstrup, Sisse Rye Ostrowski, Christopher J. O’Donnell, Matthew J. Budoff, Vilmundur Guðnason, Wendy S. Post, Jerome I. Rotter, Mark Lathrop, Henning Bundgaard, Bengt Johansson, Johan Ljungberg, Ulf Näslund, Thierry Le Tourneau, J. G. Smith, Quinn S. Wells, Stefan Söderberg, Kāri Stefánsson, Jean‐Jacques Schott, Daniel J. Rader, Robert Clarke, James C. Engert, George Thanassoulis - European Heart Journal 2023 cited by 112

  7. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jessica D. Faul, Eric B. Fauman, Cristiano Fava, Teresa Ferreira, Christopher N. Foley, Nora Franceschini, He Gao, Olga Giannakopoulou, Franco Giulianini, Daníel F. Guðbjartsson, Xiuqing Guo, Sarah E. Harris, Aki S. Havulinna, Anna Helgadóttir, Jennifer E. Huffman, Shih‐Jen Hwang, Stavroula Kanoni, Jukka Kontto, Martin G. Larson, Ruifang Li‐Gao, Jaana Lindström, Luca A. Lotta, Yingchang Lu, Jian’an Luan, Anubha Mahajan, Giovanni Malerba, Nicholas G. D. Masca, Hao Mei, Cristina Menni, Dennis O. Mook‐Kanamori, David Mosén-Ansorena, Martina Müller‐Nurasyid, Guillaume Paré, Dirk S. Paul, Markus Perola, Alaitz Poveda, Rainer Rauramaa, Melissa A. Richard, Tom G. Richardson, Nuno Sepúlveda, Xueling Sim, Albert V. Smith, Jennifer A. Smith, James R Staley, Alena Stanáková, Patrick Sulem, Sébastien Thériault, Unnur Þorsteinsdóttir, Stella Trompet, Tibor V. Varga, Digna R. Velez Edwards, Giovanni Veronesi, Stefan Weiß, Sara M. Willems, Jie Yao, Robin Young, Bing Yu, Weihua Zhang, Jinghua Zhao, Wei Zhao, Wei Zhao, Εvangelos Εvangelou, Stefanie Aeschbacher, Eralda Asllanaj, Stefan Blankenberg, Lori L. Bonnycastle, Jette Bork‐Jensen, Ivan Brandslund, Peter S. Braund, Stephen Burgess and 212 more - Nature Genetics 2020 cited by 239

  8. Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hrefna Johannsdottir, Ingileif Jónsdóttir, Thorhildur Juliusdottir, Noor Kalsheker, A. K. Kasimov, John P. Kemp, Katja Kivinen, Kari Klungsøyr, Wai Lee, Mads Melbye, Zosia Miedzybrodska, Ashley Moffett, Dilbar Najmutdinova, Firuza Nishanova, Thorunn A. Olafsdottir, Markus Perola, Fiona Broughton Pipkin, Lucilla Poston, Gordon Prescott, Saedís Saevarsdóttir, Damilya Salimbayeva, Paula J. Scaife, Line Skotte, Eleonora Staines-Urias, Ólafur Andri Stefánsson, Karina Meden Sørensen, Liv Cecilie Vestrheim Thomsen, Vinicius Tragante, Lill Trogstad, Nigel Simpson, Hannele Laivuori, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Linda Morgan, Fiona Broughton Pipkin, Noor Kalsheker, James J. Walker, Sheila Macphail, Mark D. Kilby, Marwan Habiba, Catherine Williamson, Kevin M. O’Shaughnessy, Shaughn O’Brien, Alan C. Cameron, Christopher W.G. Redman, Martin Farrall, Mark J. Caulfield, Anna F. Dominiczak, Tamara Aripova, Juan P. Casas, Anna F. Dominiczak, James J. Walker, Unnur Þorsteinsdóttir, Ann‐Charlotte Iversen, Bjarke Feenstra, Debbie A. Lawlor, Heather A. Boyd, Per Magnus, Hannele Laivuori, Nodira Zakhidova, Gulnara Svyatova, Kāri Stefánsson, Linda Morgan - Nature Communications 2020 cited by 193

  9. Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Patrick Sulem, Unnur Þorsteinsdóttir, Hilma Hólm, Daníel F. Guðbjartsson, Kāri Stefánsson - JAMA 2023 cited by 114

  10. Variants conferring risk of atrial fibrillation on chromosome 4q25

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eric E. Smith, Jonathan Rosand, Jan Hillert, Ronald C.W., Patrick T. Ellinor, Guðmundur Þorgeirsson, Jeffrey R. Gulcher, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature 2007 cited by 960

  11. Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kāri Stefánsson - Nature Genetics 2023 cited by 69

  12. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson - Nature Genetics 2016 cited by 265

  13. Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hilma Hólm, Kāri Stefánsson - Journal of the American College of Cardiology 2019 cited by 221

  14. VariantASGR1Associated with a Reduced Risk of Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Williams, André M. van Rij, Gregory T. Jones, Riyaz Patel, Allan I. Levey, Salim S. Hayek, Svati H. Shah, Muredach P. Reilly, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Lambertus A. Kiemeney, Arshed A. Quyyumi, Daniel J. Rader, William E. Kraus, Nilesh J. Samani, Oluf Pedersen, Guðmundur Þorgeirsson, Gísli Másson, Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Unnur Þorsteinsdóttir, Kāri Stefánsson - New England Journal of Medicine 2016 cited by 191

  15. Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lambertus A. Kiemeney, Oluf Pedersen, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2008 cited by 1,405

  16. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thorsten Kessler, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B. Nielsen, Markus M. Nöthen, Shichao Pang, Tobias Reinberger, Guðmar Þorleifsson, Moritz von Scheidt, Jacob K Ulirsch, Biobank Japan, Davíð O. Arnar, Deepak Atri, Noël P. Burtt, Maria C. Costanzo, Jason Flannick, Rajat M. Gupta, Kaoru Ito, Dongkeun Jang, Yoichiro Kamatani, Amit V. Khera, Issei Komuro, Iftikhar J. Kullo, Luca A. Lotta, Christopher P. Nelson, Robert Roberts, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Tom R. Webb, Aris Baras, Johan Björkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C. Morrison, Marju Orho‐Melander, Lοukianos S. Rallidis, Arno Ruusalepp, Marc S. Sabatine, Kāri Stefánsson, Pierre Zalloua, Patrick T. Ellinor, Martin Farrall, John Danesh, Christian T. Ruff, Hilary K. Finucane, Jemma C. Hopewell, Robert Clarke, Jeanette Erdmann, Nilesh J. Samani, Heribert Schunkert, Hugh Watkins, Cristen J. Willer, Panos Deloukas, Sekar Kathiresan, Adam S. Butterworth - medRxiv 2021 cited by 69

  17. Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Unnur Unnsteinsdóttir, G. Bragi Walters, Florian Zink, Linn Rødevand, Ole A. Andreassen, Jannicke Igland, Rolv T. Lie, Jan Haavik, Karina Banasik, Søren Brunak, Maria Didriksen, Mie Topholm Bruun, Christian Erikstrup, Lisette J. A. Kogelman, Kaspar René Nielsen, Erik Sørensen, Ole Birger Pedersen, Henrik Ullum, Jakob Thaning Bay, Jens Kjærgaard Boldsen, Thorsten Brodersen, Kristoffer Sølvsten Burgdorf, Khoa Manh Dinh, Joseph Dowsett, Bjarke Feenstra, Frank Geller, Lotte Hindhede, Henrik Hjalgrim, Rikke Louise Jacobsen, Gregor B. E. Jemec, Katrine Kaspersen, Bertram D. Kjerulf, Margit Anita Hørup Larsen, Ioannis Louloudis, Agnete Troen Lundgaard, Susan Mikkelsen, Christina Mikkelsen, Janna Nissen, Mette Nyegaard, Alexander Pil Henriksen, Palle Duun Rohde, Klaus Rostgaard, Michael Swinn, Lise Wegner Thørner, Mie Topholm Bruun, Thomas Werge, David Westergaard, Gísli Másson, Unnur Þorsteinsdóttir, Jes Olesen, Pétur Lúðvígsson, Ólafur Thorarensen, Anna Bjornsdottir, Gudrun R. Sigurdardottir, Ólafur Sveinsson, Sisse Rye Ostrowski, Hilma Hólm, Daníel F. Guðbjartsson, Guðmar Þorleifsson, Patrick Sulem, Hreinn Stefánsson, Thorgeir E. Thorgeirsson, Thomas Folkmann Hansen, Kāri Stefánsson - Nature Genetics 2023 cited by 55

  18. Genetics of gene expression and its effect on disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jeffrey R. Gulcher, Marc L. Reitman, Augustine Kong, Eric E. Schadt, Kāri Stefánsson - Nature 2008 cited by 1,347

  19. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Maria Samuel, John Danesh, Danish Saleheen, John C Chambers, Paul Elliott, Weihua Zhang, Weihua Zhang, John C Chambers, Jaspal S. Kooner, Mark Lathrop, Jörg Hager, Simon Heath, Marc Délepine, Kathy Stirrups, Leena Peltonen, Nicole Soranzo, Panos Deloukas, Muhammed Murtaza, Paul Elliott, John Öhrvik, Lasse Folkersen, Angela Silveira, Ferdinand M van 't Hooft, Rona J. Strawbridge, Anders Mälarstig, Per Eriksson, Anders Hamsten, John Öhrvik, Lasse Folkersen, Angela Silveira, Ferdinand M. van’t Hooft, Rona J. Strawbridge, Anders Mälarstig, Per Eriksson, Anders Hamsten, James Scott, Jaspal S. Kooner, Joban Sehmi, Rhian Gwilliam, Sarah Hunt, Sarah Edkins, Emma Gray, Suzannah Bumpstead, Simon Potter, Ann‐Christine Syvänen, Tomas Axelsson, Anders Franco-Cereceda, Anders Gabrielsen, Udo Seedorf, Stephan Rust, Gerd Assmann, Gonçalo R. Abecasis, Nabeel Ahmed, Angad S. Kooner, Mark J. Caulfield, Mark I. McCarthy, Peter Donnelly, Peter Donnelly, Philippe Froguel, Mark I McCarthy, Mark I McCarthy, N. J. Samani, N. J. Samani, Mai‐Lis Hellénius, Gunnar Olsson, Gunnar Olsson, Gianni Tognoni, Simona Barlera, Maria Grazia Franzosi, F. Gori and 32 more - Nature Genetics 2011 cited by 686

  20. Actionable Genotypes and Their Association with Life Span in Iceland

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jona Saemundsdottir, Ólafur Þ. Magnússon, Gísli Másson, Bjarni V. Halldórsson, Agnar Helgason, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Þórunn Rafnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson, Patrick Sulem - New England Journal of Medicine 2023 cited by 56

  21. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven Boonen, Dorota Włoch-Kopeć, Valerie Valant, Julia Slark, Karen L. Furie, Hossein Delavaran, Cordelia Langford, Panos Deloukas, Sarah Edkins, Sarah Hunt, Emma Gray, Serge Dronov, Leena Peltonen, Sólveig Grétarsdóttir, Gudmar Thorleifsson, Unnur Þorsteinsdóttir, Kāri Stefánsson, Giorgio B. Boncoraglio, Eugenio Parati, John Attia, Elizabeth Holliday, Christopher Levi, Maria-Grazia Franzosi, Anuj Goel, Anna Helgadóttir, Jenefer M. Blackwell, Elvira Bramon, Matthew A. Brown, Juan P. Casas, Aiden Corvin, Audrey Duncanson, Janusz Jankowski, Christopher G. Mathew, Colin N A Palmer, Robert Plomin, Anna Rautanen, Stephen Sawcer, Richard C. Trembath, Ananth C. Viswanathan, Nicholas Wood, Bradford B. Worrall, Steven J. Kittner, Braxton D. Mitchell, Brett Kissela, James F. Meschia, Vincent Thijs, Arne Lindgren, Mary Joan MacLeod, Agnieszka Słowik, James Walters, Jonathan Rosand, Pankaj Sharma, Martin Farrall, Cathie Sudlow, Peter M. Rothwell, Martin Dichgans, Peter Donnelly, Hugh S. Markus - Nature Genetics 2012 cited by 420

  22. Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2018 cited by 155

  23. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jakob Werner Hansen, Vibeke Backer, Thomas Werge, Christer Janson, Ulla‐Britt Jönsson, Maggie Ng, Juliana C.N. Chan, Wing Yee So, Ronald C.W., Svati H. Shah, Christopher B. Granger, Arshed A. Quyyumi, Allan I. Levey, Viola Vaccarino, Muredach P. Reilly, Daniel J. Rader, Michael Williams, André M. van Rij, Gregory T. Jones, Elisabetta Trabetti, Giovanni Malerba, Pier Franco Pignatti, Attilio Boner, Lydia Pescollderungg, Domenico Girelli, Oliviero Olivieri, Nicola Martinelli, Björn R. Lúdvíksson, Dóra Lúðvíksdóttir, Guðmundur I. Eyjólfsson, Davíð O. Arnar, Guðmundur Þorgeirsson, Klaus A. Deichmann, Philip J. Thompson, Matthias Wjst, Ian P. Hall, Dirkje S. Postma, Þórarinn Gíslason, Jeffrey R. Gulcher, Augustine Kong, Ingileif Jónsdóttir, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2009 cited by 762

  24. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Weang-Kee Ho, Joanna Pera, Robin Lemmens, Bo Norrving, Peter Higgins, Marianne Benn, Michèle M. Sale, Gregor Kuhlenbäumer, Alex S. F. Doney, Astrid M. Vicente, Hossein Delavaran, Ale Algra, Gail Davies, Sofia A. Oliveira, Colin N A Palmer, Ian J. Deary, Helena Schmidt, Massimo Pandolfo, Joan Montaner, Cara L. Carty, Paul I. W. de Bakker, Konstantinos Kostulas, José M. Ferro, Natalie R. van Zuydam, Einar Már Valdimarsson, Børge G. Nordestgaard, Arne Lindgren, Vincent Thijs, Agnieszka Słowik, Danish Saleheen, Guillaume Paré, Klaus Berger, Guðmar Þorleifsson, Albert Hofman, Thomas H. Mosley, Braxton D. Mitchell, Karen L. Furie, Robert Clarke, Christopher Levi, Sudha Seshadri, Andreas Gschwendtner, Giorgio B. Boncoraglio, Pankaj Sharma, Joshua C Bis, Sólveig Grétarsdóttir, Bruce M. Psaty, Peter M. Rothwell, Jonathan Rosand, James F. Meschia, Kāri Stefánsson, Martin Dichgans, Hugh S. Markus - The Lancet Neurology 2012 cited by 487